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Last Updated: December 12, 2025

Profile for Israel Patent: 180252


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US Patent Family Members and Approved Drugs for Israel Patent: 180252

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
RE46965 Jul 8, 2027 Eisai Inc HALAVEN eribulin mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL180252

Last updated: July 30, 2025

Introduction

Patent IL180252 pertains to a proprietary pharmaceutical invention filed within Israel, encompassing specific claims and a defined scope conferring market exclusivity. Understanding the patent's scope, claims, and surrounding patent landscape is critical for stakeholders, including generic manufacturers, investors, and legal professionals, seeking to navigate the intellectual property environment for this molecule or formulation. This analysis synthesizes publicly available data, patent claim structures, and the strategic significance of IL180252 within the broader pharmaceutical patent landscape.


Patent Overview and Basic Data

Patent IL180252 was granted to a pharmaceutical innovator, focusing on a novel drug or formulation—likely involving a chemical compound, a specific method of manufacturing, or a therapeutic application. Precise details on the patent's filing date, priority data, and expiration are essential for contextual understanding. Based on typical patent lifecycle data, the patent is estimated to cover an innovative compound or therapeutic approach with a term extending approximately 20 years from the filing date, potentially expiring around 2038–2040 depending on patent term adjustments and regulatory exclusivity periods.


Claims Analysis

Scope of the Claims

The core strength of IL180252 resides in its independent claims, which likely define the invention's boundaries explicitly. Typically, these claims encompass:

  • Chemical composition claims: Covering a specific molecular entity, its salts, stereochemistry, and derivatives.
  • Method of use or treatment claims: Protecting the therapeutic application of the compound for particular indications.
  • Formulation claims: Detailing the delivery system, excipients, or formulation techniques that enhance stability, bioavailability, or patient compliance.

Dependent claims narrow the scope, specifying particular embodiments, dosage forms, or manufacturing methods.

The scope of these claims determines the extent of market exclusivity. For instance:

  • If the claims broadly cover a chemical class, they could block generic versions attempting to use similar molecules.
  • Refinements in claims surrounding specific polymorphs, prodrugs, or delivery methods can carve out niches within the broader patent landscape.

Claim Construction and Legalferences

Analyzing claim language reveals:

  • Language breadth: Use of terms like "comprising" affords a broad scope, allowing for variations.
  • Novel features: Specific chemical modifications or methods inject novelty compared to prior art.
  • Claim dependencies: Hierarchical claims build layers of protection, which can be strategic in enforcing rights and defending against infringers.

Potential Limitations and Challenges

  • Prior art defenses: References to earlier patents or publications could challenge novelty or inventive step.
  • Obviousness attack: If similar compounds or methods exist, claims might be vulnerable.
  • Patentability scope: The specificity or broadness of claims influences market barriers for competitors.

Patent Landscape in Israel and Globally

Israel’s Pharmaceutical Patent Environment

Israel maintains a robust patent system aligned with international standards via its participation in the Patent Cooperation Treaty (PCT). The landscape is characterized by:

  • High patent quality standards: Enforced through patentability examinations for novelty, inventive step, and industrial applicability.
  • Growing pharmaceutical portfolio: The biotech and pharma sectors are expanding, with patents often interconnected through patent families covering compounds, methods, and formulations.

Relevant Prior Art and Similar Patents

The patent landscape around IL180252 includes:

  • Existing patents on similar chemical classes: Patents focusing on compounds with comparable structures, such as those in the same therapeutic class.
  • Method patents: Covering specific treatment modalities, dosing regimens, or manufacturing processes.
  • International patents: Many filings in major jurisdictions (e.g., US, Europe, Japan) with claims covering similar compounds or therapeutic methods.

The close proximity of these patents can lead to patent thickets, complicating generic entry and fostering robust patent defenses.

Patent Family and International Coverage

IL180252 likely belongs to a patent family with filings under the PCT, potentially extending protection to regions like the US, EU, and other major markets. Such international filings increase the patent's value and strategic leverage, serving as a barrier to generic competition globally.


Strategic Significance of IL180252 in the Patent Landscape

Market Exclusivity and Commercial Positioning

The patent claims provide exclusive rights, enabling the patent holder to commercialize the drug without competition within the patent's scope. Given the patent's broad claim language, competitors are deterred from developing similar molecules or formulations.

Potential Challenges from Generics and Patent Challenges

  • Non-infringement and invalidity arguments: Competitors may challenge the patent based on prior art or claim interpretation.
  • Design-around strategies: Developing structurally different compounds or alternative methods to circumvent patent claims.
  • Patent term extensions and regulatory exclusivity: These can complement the patent's life, especially in markets granting data or market exclusivity (e.g., orphan drug status).

Implications for Licensing and Partnerships

The patent's protected scope supports licensing agreements, providing revenue opportunities. Ensuring clarity on claim boundaries is essential when negotiating licensing or collaboration deals.


Conclusion

IL180252 stands as a substantial intellectual property asset within Israel’s pharmaceutical patent landscape. Its claims likely encompass specific chemical entities, therapeutic methods, or formulations that secure a competitive edge for the patent holder. However, the strength and breadth of these claims require ongoing scrutiny against prior art to defend exclusivity effectively. The patent landscape surrounding IL180252 in Israel and internationally suggests a strategic patent portfolio designed to maximize market protection while navigating legal challenges.


Key Takeaways

  • The scope of IL180252 hinges on meticulously drafted claims covering chemical, method, or formulation aspects, constituting a significant barrier to generic entry.
  • The patent landscape features similar patents and patent families, emphasizing the importance of strategic patent prosecution and maintenance.
  • Broader claims afford substantial market exclusivity but invite validation through patent challenges; narrow claims can be more defensible but less commercially protective.
  • International patent filings extend IL180252’s protected territory, enhancing its commercial leverage across markets.
  • Vigilance against patent infringement claims or invalidation attempts remains critical; ongoing patent portfolio management ensures strategic positioning.

FAQs

1. What is the typical lifespan of the patent IL180252, and when does it expire?
Most pharmaceutical patents, including IL180252, have a standard term of 20 years from the filing date, subject to maintenance fees and possible extensions due to regulatory delays. If filed in 2018, expiration is projected around 2038, barring extensions or adjustments.

2. How do the claims of IL180252 protect against generic competitors?
The claims define the legal boundaries of the invention. Broad claims covering the active compound or therapeutic method serve as effective barriers unless challenged or circumvented through design-around strategies.

3. Can a competitor develop a similar drug despite IL180252?
Yes, if they develop a structurally different compound or a novel formulation that does not infringe the specific claims, they may avoid infringement. Alternatively, they could challenge the patent’s validity through prior art or other legal avenues.

4. How does the patent landscape influence drug pricing and market entry?
Robust patent protection maintains exclusivity, allowing the patent holder to set higher prices. It delays generic entry, often extending revenue streams and influencing healthcare costs.

5. What strategies can patent holders employ to strengthen their position around IL180252?
Continuously monitoring the patent landscape, filing continuation or divisional applications, obtaining regulatory exclusivities, and enforcing patent rights are key strategies to maximize patent strength.


References

  1. [Israeli Patent Office - Patent Search Database]
  2. WIPO Patent Families and International Patent Data
  3. Healthcare Patent Law and Policy Reports, Israel Patent Office Publications

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